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RNA 指导的 DNA 甲基化途径和组蛋白乙酰转移酶在拟南芥中的抗沉默作用。

Antisilencing role of the RNA-directed DNA methylation pathway and a histone acetyltransferase in Arabidopsis.

机构信息

State Key Laboratory of Plant Physiology and Biochemistry, College of Biological Sciences, China Agricultural University, Beijing 100193, China.

出版信息

Proc Natl Acad Sci U S A. 2012 Jul 10;109(28):11425-30. doi: 10.1073/pnas.1208557109. Epub 2012 Jun 25.

Abstract

REPRESSOR OF SILENCING 1 (ROS1) is a DNA demethylation enzyme that was previously identified during a genetic screen for the silencing of both RD29A-LUC and 35S-NPTII transgenes on a T-DNA construct. Here we performed a genetic screen to identify additional mutants in which the 35S-NPTII transgene is silenced. We identified several alleles of ros1 and of the following components of the RNA-directed DNA methylation (RdDM) pathway: NRPD1 (the largest subunit of polymerase IV), RDR2, NRPE1 (the largest subunit of polymerase V), NRPD2, AGO4, and DMS3. Our results show that the silencing of 35S-NPTII in the RdDM pathway mutants is due to the reduced expression of ROS1 in the mutants. We also identified a putative histone acetyltransferase (ROS4) from the genetic screen. The acetyltransferase contains a PHD-finger domain that binds to unmethylated histone H3K4. The mutation in ROS4 led to reduction of H3K18 and H3K23 acetylation levels. We show that the silencing of 35S-NPTII and some transposable element genes was released by the ddm1 mutation but that this also required ROS4. Our study identifies a unique antisilencing factor, and reveals that the RdDM pathway has an antisilencing function due to its role in maintaining ROS1 expression.

摘要

沉默抑制因子 1(ROS1)是一种 DNA 去甲基化酶,它是在一个 T-DNA 构建体上对 RD29A-LUC 和 35S-NPTII 转基因的沉默进行遗传筛选时发现的。在这里,我们进行了遗传筛选,以鉴定其他沉默 35S-NPTII 转基因的突变体。我们鉴定了 ros1 的几个等位基因,以及 RNA 指导的 DNA 甲基化(RdDM)途径的以下成分的等位基因:NRPD1(聚合酶 IV 的最大亚基)、RDR2、NRPE1(聚合酶 V 的最大亚基)、NRPD2、AGO4 和 DMS3。我们的结果表明,RdDM 途径突变体中 35S-NPTII 的沉默是由于突变体中 ROS1 的表达减少所致。我们还从遗传筛选中鉴定了一个假定的组蛋白乙酰转移酶(ROS4)。该乙酰转移酶包含一个 PHD 指结构域,该结构域与未甲基化的组蛋白 H3K4 结合。ROS4 中的突变导致 H3K18 和 H3K23 乙酰化水平降低。我们表明,ddm1 突变释放了 35S-NPTII 和一些转座元件基因的沉默,但这也需要 ROS4。我们的研究鉴定了一个独特的抗沉默因子,并揭示了 RdDM 途径由于其维持 ROS1 表达的作用而具有抗沉默功能。

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